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在超级启动子的作用下过表达 3-羟-3-甲基戊二酰基辅酶 A 还原酶 1(hmgr1)基因以提高橡胶树(Hevea brasiliensis Muell. Arg.)乳胶生物合成。

Over-expression of 3-hydroxy-3- methylglutaryl-coenzyme A reductase 1 (hmgr1) gene under super-promoter for enhanced latex biosynthesis in rubber tree (Hevea brasiliensis Muell. Arg.).

机构信息

Advanced Center for Molecular Biology and Biotechnology, Rubber Research Institute of India, Kottayam 686 009, Kerala, India.

Department of Bioinformatics, Centre for Plant Biotechnology Molecular Biology, Kerala Agricultural University, Thrissur, Kerala, India.

出版信息

Plant Physiol Biochem. 2018 Jun;127:414-424. doi: 10.1016/j.plaphy.2018.04.011. Epub 2018 Apr 13.

Abstract

Natural rubber (cis-1, 4-polyisoprene) is being produced from bark laticifer cells of Hevea brasiliensis and the popular high latex yielding Indian rubber clones are easily prone to onset of tapping panel dryness syndrome (TPD) which is considered as a physiological syndrome affecting latex production either partially or completely. This report describes an efficient protocol for development of transgenic rubber plants by over-expression of 3-hydroxy 3-methylglutaryl Co-enzyme A reductase 1 (hmgr1) gene which is considered as rate limiting factor for latex biosynthesis via Agrobacterium-mediated transformation. The pBIB plasmid vector containing hmgr1 gene cloned under the control of a super-promoter was used for genetic transformation using embryogenic callus. Putatively transgenic cell lines were obtained on selection medium and produced plantlets with 44% regeneration efficiency. Transgene integration was confirmed by PCR amplification of 1.8 kb hmgr1 and 0.6 kb hpt genes from all putatively transformed callus lines as well as transgenic plants. Southern blot analysis showed the stable integration and presence of transgene in the transgenic plants. Over expression of hmgr1 transgene was determined by Northern blot hybridization, semi-quantitative PCR and real-time PCR (qRT-PCR) analysis. Accumulation of hmgr1 mRNA transcripts was more abundant in transgenic plants than control. Increased level of photosynthetic pigments, protein contents and HMGR enzyme activity was also noticed in transgenic plants over control. Interestingly, the latex yield was significantly enhanced in all transgenic plants compared to the control. The qRT-PCR results exhibit that the hmgr1 mRNA transcript levels was 160-fold more abundance in transgenic plants over untransformed control. These results altogether suggest that there is a positive correlation between latex yield and accumulation of mRNA transcripts level as well as HMGR enzyme activity in transgenic rubber plants. It is presumed that there is a possibility for enhanced level of latex biosynthesis in transgenic plants as the level of mRNA transcripts and HMGR enzyme activity is directly correlated with latex yield in rubber tree. Further, the present results clearly suggest that the quantification of HMGR enzyme activity in young seedlings will be highly beneficial for early selection of high latex yielding plants in rubber breeding programs.

摘要

天然橡胶(顺式-1,4-聚异戊二烯)是从巴西橡胶树的树皮乳管细胞中提取的,而高产胶的印度橡胶克隆品很容易患上割胶面板干燥症(TPD),这被认为是一种影响乳胶生产的生理综合征,无论是部分还是完全。本报告描述了一种通过过表达 3-羟基-3-甲基戊二酰辅酶 A 还原酶 1(hmgr1)基因来开发转基因橡胶植物的有效方案,该基因被认为是通过根瘤农杆菌介导的转化影响乳胶生物合成的限速因素。pBIB 质粒载体包含 hmgr1 基因,该基因在超级启动子的控制下克隆,用于利用胚性愈伤组织进行遗传转化。在选择培养基上获得了推定的转基因细胞系,并以 44%的再生效率产生了植株。通过对所有推定转化的愈伤组织系以及转基因植物中 1.8kb hmgr1 和 0.6kb hpt 基因的 PCR 扩增,证实了转基因的整合。Southern blot 分析显示,转基因植物中存在稳定的整合和转基因的存在。通过 Northern blot 杂交、半定量 PCR 和实时 PCR(qRT-PCR)分析,确定了 hmgr1 转基因的过表达。在转基因植物中,hmgr1 mRNA 转录本的积累比对照更为丰富。在转基因植物中,还注意到光合色素、蛋白质含量和 HMGR 酶活性的增加。有趣的是,与对照相比,所有转基因植物的乳胶产量都显著提高。qRT-PCR 结果表明,与未转化对照相比,转基因植物中 hmgr1 mRNA 转录本的丰度增加了 160 倍。这些结果表明,在转基因橡胶植物中,乳胶产量与 mRNA 转录本水平和 HMGR 酶活性之间存在正相关关系。可以推测,由于 mRNA 转录本和 HMGR 酶活性与橡胶树中的乳胶产量直接相关,因此转基因植物中可能存在增强乳胶生物合成的可能性。此外,本研究结果清楚地表明,在橡胶树的早期选择中,对幼苗中 HMGR 酶活性的定量将非常有益。

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